Evidence map›Paper›PMID 36350810›Full record

ArticlePloS one2022

Primary hypertension, anti-hypertensive medications and the risk of severe COVID-19 in UK Biobank.

Holly Pavey, Spoorthy Kulkarni, Angela Wood, Yoav Ben-Shlomo, Peter Sever, Carmel McEniery, Ian Wilkinson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Holly PaveyDivision of Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-5014-5118
Spoorthy KulkarniDepartment of Clinical Pharmacology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.ORCID 0000-0003-2827-214X
Angela WoodBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Yoav Ben-ShlomoPopulation Health Sciences, University of Bristol, Bristol, United Kingdom.
Peter SeverNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Carmel McEnieryDivision of Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge, United Kingdom.
Ian WilkinsonDivision of Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBCambridge University Hospitals NHS Foundation Trust · GBImperial College London · GBUniversity of Bristol · GB

Funding

British Heart Foundation RG/13/13/30194British Heart Foundation RG/18/13/33946Department of Health BRC-1215-20014Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MR/L003120/1
6 · The paper itself

Abstract

Hypertension appears to be one of the commonest comorbidities in COVID-19 patients, although whether hypertensive individuals have a higher risk of severe COVID-19 compared with non-hypertensives is unclear. It is also unclear whether the absolute level of systolic blood pressure, or the type of anti-hypertensive medication is related to this risk. Analyses were conducted using data from the UK Biobank and linked health records. Logistic regression models were fitted to assess the impact of hypertension, systolic blood pressure (SBP) and medications on the risk of severe COVID-19. 16,134 individuals tested positive for severe acute respiratory syndrome-coronavirus, 22% (n = 3,584) developed severe COVID-19 and 40% (n = 6,517) were hypertensive. Hypertension was associated with 22% higher odds of severe COVID-19 (Odds ratio (OR) 1.22; 95% confidence interval (CI) 1.12, 1.33), compared with normotension after adjusting for confounding variables. In those taking anti-hypertensive medications, elevated SBP showed a dose-response relationship with severe COVID-19 (150-159mmHg versus 120-129mmHg (OR 1.91; 95% CI 1.44, 2.53), >180+mmHg versus 120-129mmHg (OR 1.93; 95% CI 1.06, 3.51)). SBP <120mmHg was associated with greater odds of severe COVID-19 (OR 1.40; 95% CI 1.11, 1.78). Angiotensin-converting enzyme inhibitors or angiotensin-II receptor blockers were not associated with altered risk of severe COVID-19. Hypertension is an important risk factor for COVID-19. A better understanding of the underlying mechanisms is warranted in case of more severe strains or other viruses in the future.

Indexed as

COVID-19HypertensionAngiotensin Receptor AntagonistsAntihypertensive AgentsBiological Specimen BanksHumansRetrospective StudiesUnited KingdomAngiotensin Receptor AntagonistsAntihypertensive Agents

Identifiers

PMID36350810
PMCPMC9645600
OpenAlexW4308623293

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.